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Sodium Bicarbonate
Sodium Bicarbonate - 52584-900-34 - (Sodium Bicarbonate)
Drug Information of Sodium Bicarbonate
| Product NDC: | 52584-900 |
| Proprietary Name: | Sodium Bicarbonate |
| Non Proprietary Name: | Sodium Bicarbonate |
| Active Ingredient(s): | 1 meq/mL & nbsp; Sodium Bicarbonate |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Sodium Bicarbonate
| Product NDC: | 52584-900 |
| Labeler Name: | General Injectables & Vaccines, Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20100801 |
Package Information of Sodium Bicarbonate
| Package NDC: | 52584-900-34 |
| Package Description: | 1 BOX in 1 BAG (52584-900-34) > 1 SYRINGE, GLASS in 1 BOX > 10 mL in 1 SYRINGE, GLASS |
NDC Information of Sodium Bicarbonate
| NDC Code | 52584-900-34 |
| Proprietary Name | Sodium Bicarbonate |
| Package Description | 1 BOX in 1 BAG (52584-900-34) > 1 SYRINGE, GLASS in 1 BOX > 10 mL in 1 SYRINGE, GLASS |
| Product NDC | 52584-900 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Sodium Bicarbonate |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20100801 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | General Injectables & Vaccines, Inc |
| Substance Name | SODIUM BICARBONATE |
| Strength Number | 1 |
| Strength Unit | meq/mL |
| Pharmaceutical Classes |
